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25465 Alpha-2 Plasmin Inhibitor, Plasma (A2PI)

Alpha-2 Plasmin Inhibitor, Plasma (A2PI)
Test Code: A2APSO
Synonyms/Keywords

Alpha 2 Plasmin Inhibitor
Antiplasmin
Antiplasmin, Functional, Plasma
Functional Antiplasmin
Plasmin Inhibitor

Useful For

Diagnosing congenital alpha-2 plasmin inhibitor deficiencies (rare)

Providing a more complete assessment of disseminated intravascular coagulation, intravascular coagulation and fibrinolysis, or hyperfibrinolysis (primary fibrinolysis), when measured in conjunction with fibrinogen, fibrin D-dimer, fibrin degradation products, soluble fibrin monomer complex, and plasminogen

Evaluating liver disease

Evaluating the effects of fibrinolytic or antifibrinolytic therapy

Specimen Requirements
Fasting Required Specimen Type Preferred Container/Tube Acceptable Container/Tube Specimen Volume Specimen Minimum Volume
(allows for 1 repeat)
Pediatric Minimum Volume
(no repeat)
​No ​Platelet-poor Plasma ​Citrated Blue Top Tube (BTT) ​1.0 mL ​0.5 mL
Collection Processing Instructions
​1. Spin down, remove plasma, and spin plasma again.
2. Freeze specimen immediately at < or =-40 degrees C, if possible.
 
Additional Information:
1. Double-centrifuged specimen is critical for accurate results as platelet contamination may cause spurious results.
2. Each coagulation assay requested should have its own vial.
Specimen Stability Information
Specimen Type Temperature Time
​Citrated Plasma ​Frozen ​14 days
Rejection Criteria
Gross Hemolyis
Gross Lipemia
Gross Icterus
Interference

​Alpha-2 plasmin inhibitor results are potentially affected by:

-Heparin, unfractioned or low-molecular-weight >4 U/mL

-Alpha-2-macroglobulin >7 mg/mL; potentially leading to falsely-increased result

-Hemoglobin >200 mg/dL

-Bilirubin >20 mg/dL

-Triglycerides >1,000 mg/dL

Performing Laboratory Information
Performing Location Day(s) Test Performed Analytical Time Methodology/Instrumentation
​Mayo Clinic Laboratories ​Monday through Friday ​3 to 7 days ​Chromogenic
Reference Lab
Test Information
Alpha-2 plasmin inhibitor (antiplasmin) is synthesized in the liver with a biological half-life of approximately 3 days. It inactivates plasmin, the primary fibrinolytic enzyme responsible for remodeling the fibrin thrombus, and binds fibrin, together with factor XIIIa, making the clot more difficult to lyse. Absence of alpha-2 plasmin inhibitor results in uncontrolled plasmin-mediated breakdown of the fibrin clot and is associated with increased risk of bleeding.
Reference Range Information
Adults: 80-140%
Normal, full-term and premature infants may have mildly decreased levels (> or =50%) which reach adult levels < or = 90 days postnatal.* 
Interpretation
​Patients with congenital homozygous deficiency (with levels of <10%) are clinically affected (bleeding). Heterozygotes having levels of 30% to 60% of mean normal activity are usually asymptomatic.
 
Lower than normal levels may be suggestive of consumption due to activation of plasminogen and its inhibition by alpha-2 plasmin inhibitor.
 
The clinical significance of high levels of alpha-2 plasmin inhibitor is unknown.
Outreach CPTs
CPT Modifier
(if needed)
Quantity Description Comments
85410​
Synonyms/Keywords

Alpha 2 Plasmin Inhibitor
Antiplasmin
Antiplasmin, Functional, Plasma
Functional Antiplasmin
Plasmin Inhibitor

Ordering Applications
Ordering Application Description
If the ordering application you are looking for is not listed, contact your local laboratory for assistance.
Specimen Requirements
Fasting Required Specimen Type Preferred Container/Tube Acceptable Container/Tube Specimen Volume Specimen Minimum Volume
(allows for 1 repeat)
Pediatric Minimum Volume
(no repeat)
​No ​Platelet-poor Plasma ​Citrated Blue Top Tube (BTT) ​1.0 mL ​0.5 mL
Collection Processing
​1. Spin down, remove plasma, and spin plasma again.
2. Freeze specimen immediately at < or =-40 degrees C, if possible.
 
Additional Information:
1. Double-centrifuged specimen is critical for accurate results as platelet contamination may cause spurious results.
2. Each coagulation assay requested should have its own vial.
Specimen Stability Information
Specimen Type Temperature Time
​Citrated Plasma ​Frozen ​14 days
Rejection Criteria
Gross Hemolyis
Gross Lipemia
Gross Icterus
Interference

​Alpha-2 plasmin inhibitor results are potentially affected by:

-Heparin, unfractioned or low-molecular-weight >4 U/mL

-Alpha-2-macroglobulin >7 mg/mL; potentially leading to falsely-increased result

-Hemoglobin >200 mg/dL

-Bilirubin >20 mg/dL

-Triglycerides >1,000 mg/dL

Useful For

Diagnosing congenital alpha-2 plasmin inhibitor deficiencies (rare)

Providing a more complete assessment of disseminated intravascular coagulation, intravascular coagulation and fibrinolysis, or hyperfibrinolysis (primary fibrinolysis), when measured in conjunction with fibrinogen, fibrin D-dimer, fibrin degradation products, soluble fibrin monomer complex, and plasminogen

Evaluating liver disease

Evaluating the effects of fibrinolytic or antifibrinolytic therapy

Reference Range Information
Adults: 80-140%
Normal, full-term and premature infants may have mildly decreased levels (> or =50%) which reach adult levels < or = 90 days postnatal.* 
Interpretation
​Patients with congenital homozygous deficiency (with levels of <10%) are clinically affected (bleeding). Heterozygotes having levels of 30% to 60% of mean normal activity are usually asymptomatic.
 
Lower than normal levels may be suggestive of consumption due to activation of plasminogen and its inhibition by alpha-2 plasmin inhibitor.
 
The clinical significance of high levels of alpha-2 plasmin inhibitor is unknown.
For more information visit:
Performing Laboratory Information
Performing Location Day(s) Test Performed Analytical Time Methodology/Instrumentation
​Mayo Clinic Laboratories ​Monday through Friday ​3 to 7 days ​Chromogenic
Reference Lab
For billing questions, see Contacts
Outreach CPTs
CPT Modifier
(if needed)
Quantity Description Comments
85410​
For most current information refer to the Marshfield Laboratory online reference manual.